Senior Clinical Research Associate as a Lead Monitor is responsible for the compliance and oversight of clinical trials that implement a Risk-Based Monitoring (RBM) strategy and being the main point of contact between the study team and site monitors. The role includes performing study compliance oversight by conducting Site Compliance Meetings, analyzing data to identify potential compliance outliers, and working with study teams and sites to resolve identified issues. The lead monitor may also provide Site Management input to the study team throughout all study phases, including study design, start
